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Publications by Michio Hirano

Mitochondrial Diseases in North America

Neurology: Genetics
NeurologyGenetics
2020English

Nuclear Localization of SMN and FUS Is Not Altered in Fibroblasts From Patients With Sporadic ALS

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
MedicineNeurology
2014English

Slowly Progressive Encephalopathy With Hearing Loss Due to a Mutation in the mtDNA tRNALeu(CUN) Gene

Journal of the Neurological Sciences
Neurology
2010English

Treatment of CoQ10 Deficient Fibroblasts With Ubiquinone, CoQ Analogs, and Vitamin C: Time- And Compound-Dependent Effects

PLoS ONE
Multidisciplinary
2010English

Mutation in an mtDNA Protein-Coding Gene

Journal of Child Neurology
Child HealthNeurologyPediatricsPerinatology
2012English

Assessment of Thymidine Phosphorylase Function: Measurement of Plasma Thymidine (And Deoxyuridine) and Thymidine Phosphorylase Activity

Methods in Molecular Biology
GeneticsMolecular Biology
2011English

A Novel POLG Gene Mutation in a Patient With SANDO

Journal of Experimental and Integrative Medicine
Alternative MedicineComplementary
2012English

Mitochondrial Myopathies

2011English

Respiratory Chain Dysfunction and Oxidative Stress Correlate With Severity of Primary CoQ10 Deficiency

FASEB Journal
BiochemistryBiotechnologyGeneticsMolecular BiologyMedicine
2008English

Advancements in the Pathophysiology of Friedreich’s Ataxia and New Prospects for Treatments

Molecular Genetics and Metabolism
GeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2007English

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